Prednisone (Page 3 of 3)

HOW SUPPLIED

Product: 50090-3330

NDC: 50090-3330-0 20 TABLET in a BOTTLE

NDC: 50090-3330-1 12 TABLET in a BOTTLE

NDC: 50090-3330-5 14 TABLET in a BOTTLE

NDC: 50090-3330-7 15 TABLET in a BOTTLE

NDC: 50090-3330-2 6 TABLET in a BOTTLE

Product: 50090-3354

Prednisone

Label ImageLabel Image

Prednisone

Label ImageLabel Image
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-3330(NDC:59746-175)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISONE (PREDNISONE) PREDNISONE 20 mg
Inactive Ingredients
Ingredient Name Strength
Lactose monohydrate
Magnesium stearate
Sodium lauryl sulfate
Fd&c Yellow No. 6
Aluminum Oxide
Starch, Corn
Starch, Potato
Product Characteristics
Color PINK (Peach) Score 2 pieces
Shape ROUND Size 11mm
Flavor Imprint Code TL175
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-3330-7 15 TABLET in 1 BOTTLE None
2 NDC:50090-3330-2 6 TABLET in 1 BOTTLE None
3 NDC:50090-3330-1 12 TABLET in 1 BOTTLE None
4 NDC:50090-3330-5 14 TABLET in 1 BOTTLE None
5 NDC:50090-3330-0 20 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040362 08/29/2001
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-3354(NDC:59746-172)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISONE (PREDNISONE) PREDNISONE 5 mg
Inactive Ingredients
Ingredient Name Strength
Lactose monohydrate
Magnesium stearate
Sodium lauryl sulfate
Starch, Corn
Starch, Potato
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code TL172
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-3354-7 60 TABLET in 1 BOTTLE None
2 NDC:50090-3354-1 50 TABLET in 1 BOTTLE None
3 NDC:50090-3354-3 100 TABLET in 1 BOTTLE None
4 NDC:50090-3354-0 21 TABLET in 1 BOTTLE, PLASTIC None
5 NDC:50090-3354-4 30 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040362 08/29/2001 12/31/2019
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-3330), REPACK (50090-3330), RELABEL (50090-3354), REPACK (50090-3354)

Revised: 08/2022 A-S Medication Solutions

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